Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion type Assertion NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_head.
- NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion description "[Therefore, ZNF127 and ZNF127AS are novel imprinted genes that may be associated with some of the clinical features of the polygenic Prader-Willi syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_provenance.
- NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion evidence source_evidence_literature NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_provenance.
- NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion SIO_000772 10196367 NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_provenance.
- NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion wasDerivedFrom befree-2016 NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_provenance.
- NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_assertion wasGeneratedBy ECO_0000203 NP249678.RAumuVCbYE-zpaUzZLw7AJqWdpB0eL-T7LViZDl8eT8_4130_provenance.